
Senior Clinical Research Associate
Posted Oct 28

Posted Oct 28
This is a fully remote position, open to applicants in Oregon.
• Conduct on-site or remote monitoring visits for Pre-Study, Initiation, Interim, and Close-Out phases.
• Ensure that investigational facilities and personnel are sufficiently equipped for study implementation.
• Identify and assess investigators, confirming their qualifications, resources, facilities, equipment, and staff.
• Provide training to investigational site staff as needed.
• Assist in the preparation of regulatory and/or Ethics Committee submissions when applicable.
• Engage in mentoring and training of new team members.
• Carry out co-monitoring visits to evaluate the performance of junior staff.
• Bachelor's or Master's degree in Life Sciences or an equivalent combination of education, training, and experience.
• Significant on-site monitoring experience in Phase 2/3 clinical trials.
• Preferably, experience with complex trials in oncology or rare diseases.
• Proficient in English with full working capability.
• Strong planning, multitasking, and teamwork abilities in a dynamic environment.
• Excellent communication, collaboration, and problem-solving skills.
• Willingness to travel nationally.
• Option for remote work.
• Opportunities for mentoring and training.
• A collaborative team atmosphere.
• Chance to contribute to pharmaceutical treatments that positively impact patients.
• A diverse and inclusive workplace.
• Opportunities for career advancement.
ICON plc
ICON plc
ICON plc
Worldwide Clinical Trials
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